Senior Technical Writer

Job Description

As an experienced technical writer at P360, your role will be crucial in enhancing our customer/client-focused services. You will need to have proven expertise in technical fields such as software development, computer science, engineering, or writing documentation in regulated environments. Your ability to analyze complex information and simplify it for others will be essential in this role.**Key Responsibilities:**- Strong writing and editing skills with meticulous attention to detail- Deep understanding of regulatory requirements (FDA, ICH) for creating documentation in regulated environments- Proficiency in MS Office tools like Word, Visio, and SharePoint- Managing projects, collaborating with subject matter experts (SMEs), and meeting deadlines in high-pressure pharma/biotech environments- Developing comprehensive documentation meeting organizational standards- Translating complex information into simple, polished, and engaging content- Writing user-friendly content to meet the audiences needs- Developing and maintaining detailed databases of reference materials- Evaluating existing content and suggesting innovative approaches for improvement**Qualifications Required:**- Bachelors degree in a relevant technical field- 5 years of industry experience as a technical writer- Experience writing documentation in a GxP environment and for validated applications- Strong understanding of GxP regulations, FDA regulations, and compliance standards- Meticulous attention to detail and accuracy- Ability to quickly learn and understand complex topics- Superior written and verbal communication skills- Experience in collaborating with engineering teams to enhance user experienceThe company, P360, offers a work-from-home opportunity, a Flexi Week culture, fixed internet allowance, and other benefits to its employees.Please note that P360 will reach out to candidates who match the current requirements. If not contacted, your information and resume will be stored for future vacancies. As an experienced technical writer at P360, your role will be crucial in enhancing our customer/client-focused services. You will need to have proven expertise in technical fields such as software development, computer science, engineering, or writing documentation in regulated environments. Your ability to analyze complex information and simplify it for others will be essential in this role.**Key Responsibilities:**- Strong writing and editing skills with meticulous attention to detail- Deep understanding of regulatory requirements (FDA, ICH) for creating documentation in regulated environments- Proficiency in MS Office tools like Word, Visio, and SharePoint- Managing projects, collaborating with subject matter experts (SMEs), and meeting deadlines in high-pressure pharma/biotech environments- Developing comprehensive documentation meeting organizational standards- Translating complex information into simple, polished, and engaging content- Writing user-friendly content to meet the audiences needs- Developing and maintaining detailed databases of reference materials- Evaluating existing content and suggesting innovative approaches for improvement**Qualifications Required:**- Bachelors degree in a relevant technical field- 5 years of industry experience as a technical writer- Experience writing documentation in a GxP environment and for validated applications- Strong understanding of GxP regulations, FDA regulations, and compliance standards- Meticulous attention to detail and accuracy- Ability to quickly learn and understand complex topics- Superior written and verbal communication skills- Experience in collaborating with engineering teams to enhance user experienceThe company, P360, offers a work-from-home opportunity, a Flexi Week culture, fixed internet allowance, and other benefits to its employees.Please note that P360 will reach out to candidates who match the current requirements. If not contacted, your information and resume will be stored for future vacancies.

Keyskills :
software developmentcomputer scienceengineeringMS Office toolsregulatory requirementsICHproject managementcollaborationcontent developmentinformation architectureSDLCtechnical writerwriting documentationFDAGxP environmentGxP regulationsFDA